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EpiVax Secures Additional Funding from FDA for Immunogenicity Risk Assessment for Biosimilar Products

EpiVax Secures Additional Funding from FDA for Immunogenicity Risk Assessment for Biosimilar Products

by Elena Iemma | Sep 12, 2022 | News

PROVIDENCE, RI, September 12, 2022 /PRNewswire/ — EpiVax, Inc. (“EpiVax”) is pleased to announce the award of a two-year, $2 million grant from the FDA’s Office of Center for Drug Evaluation and Research (CDER) to validate a method for immunogenicity risk...
EpiVax Secures Additional Funding from FDA for Immunogenicity Risk Assessment for Biosimilar Products

Immunogenicity Expert and FDA Alum Dr. Amy Rosenberg Joins EpiVax

by Elena Iemma | Jul 6, 2021 | News

PROVIDENCE, RI, July 6, 2021 /PRNewswire/ — EpiVax, Inc. (“EpiVax”) is pleased to announce that Dr. Amy Rosenberg is leaving the FDA’s Division of Therapeutic Proteins, CDER, which she led for over 20 years, to join EpiVax as Senior Director of Immunology and...
EpiVax Secures Additional Funding from FDA for Immunogenicity Risk Assessment for Biosimilar Products

EpiVax Reports Record Year for Immunogenicity Screening Toolkit (ISPRI)

by Adam | Dec 15, 2020 | News

PROVIDENCE, RI, December 15, 2020 /PRNewswire/ — EpiVax, Inc. reports a record-breaking year for the “ISPRI” immunogenicity screening toolkit. More pharmaceutical and biotechnology companies signed new and continuing licenses for access to the toolkit in 2020...

Recent Posts

  • EpiVax Announces Laboratory Expansion and Streamlined, NAM-Centric In Vitro Services    
  • Replacing Animal Models with Human-Relevant New Approach Methodologies (NAMs) for Immunogenicity in Clinic
  • EpiVax Enters its Next Chapter with SV Health Investors
  • Immunogenicity Risk Assessment Outputs to Drive a Streamlined, Risk-Based Preclinical and Clinical Strategy
  • Immunogenicity Risk Assessment Outputs to Drive a Streamlined, Risk-Based Preclinical and Clinical Strategy

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